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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1974503생성일: 2026년 10월 26일

Triphenylphosphine → HCID 54247816, 화합물

https://huagongshe.com/reaction/1974503

반응식

참여 물질

역할이름HCID투입량
반응물TriphenylphosphineHCID 11776—
반응물HydroxypropyleneHCID 143500—
반응물ethyl N-ethoxycarbonyliminocarbamateHCID 220568—
반응물2-Propen-1-ol, 3-(3-pyridinyl)-HCID 3563504—
반응물3-[1-Methoxy-1-(1,3-thiazol-2-yl)propyl]phenolHCID 15637379—
용매TetrahydrofuranHCID 8028—
생성물HCID 54247816HCID 5424781629.8%

반응 단계

Diethyl azodicarboxylate (0.38 ml) was added dropwise to a mixture of 2-[1-(3-hydroxyphenyl)-1-methoxypropyl]thiazole (0.37 g), triphenylphosphine (0.57 g), 3-(3-pyridyl)prop-2-en-1-ol (0.27 g) and tetrahydrofuran (7 ml) which had been cooled to 0°-5° C. in an ice-bath. The mixture was stirred at this temperature range for 2 hours and then at ambient temperature for 4 hours. Further portions of diethyl azodicarboxylate (0.1 ml), triphenylphosphine (0.14 g) and the propenol (0.045 g) were added and the mixture was stirred at ambient temperature for 18 hours. The mixture was partitioned between ethyl acetate (40 ml) and dilute aqueous hydrochloric acid (40 ml). The aqueous layer was separated and basified by adding potassium carbonate portionwise. The resulting solution was extracted with ethyl acetate (3×20 ml). The combined extracts were dried (Na2SO4) and evaporated. The residue was purified by column chromatography eluting with toluene/ethyl acetate (2/3 v/v) to give 2-[1-[3-(3-(3-pyridyl)prop-2-en-1-yloxy)phenyl]-1-methoxypropyl]thiazole as a colourless oil (0.162 g).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05283245
출처 데이터셋uspto-grants-1994_02
ORD IDord-3a37733dfc334c7c8d9e673541536018
출처 메모uspto-grants-1994_02